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临床试验/NL-OMON50955
NL-OMON50955已完成不适用

Immediate Stimulation to Prevent and Inhibit cardiorespiratory Events in preterm infants - InSPIRE

eids Universitair Medisch Centrum0 个研究点目标入组 16 人开始时间: 待定最近更新:

试验速览

阶段
不适用
状态
已完成
入组人数
16

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
0 至 0(—)

入选标准

  • Born between 24 weeks 0 days and 29 weeks and 6 days gestation.
  • Receiving non-invasive respiratory support (NCPAP or NIPPV).
  • Occurrence of apnea, bradycardia or desaturation of >10 seconds > 1 per hour,
  • but otherwise clinically stable.
  • Expected to complete the 48-hour period with non-invasive respiratory support.
  • Written informed parental consent.

排除标准

  • Major congenital anomalies that have an adverse effect on breathing or
  • ventilation.
  • Suspected or proven sepsis
  • Comfort score >14; comfort is scored by a nurse on 6 items with a 5-point
  • Likert scale. When the sum of these scores is >14 the patient is experiencing
  • discomfort which requires the nurse to look for the cause and, in case it does
  • not improve, provide pain medication.

研究者

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